VEINPREP VEIN GRAFT PREP. KIT A277723— 510(k) K830150

Name: FDA 510(k) clearance K830150
Creator: U.S. Food and Drug Administration
Published: 1983-02-28

Substantially Equivalent

Atrium Medical Corp.

FDA 510(k) clearance K830150 for VEINPREP VEIN GRAFT PREP. KIT A277723, Substantially Equivalent on 1983-02-28. Applicant: Atrium Medical Corp.. Device class: 2.

Clearance details

Applicant: Atrium Medical Corp.
Product code: Code DWD
Device class: Class 2
Regulation: 21 CFR 870.4430
Advisory panel: Cardiovascular
Date received: 1983-01-17
Decision date: 1983-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.